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Scott Med J ; 57(4): 217-20, 2012 Nov.
Article de Anglais | MEDLINE | ID: mdl-23002158

RÉSUMÉ

The expected duration of initial antiparkinson monotherapy before the need for supplementation is not clearly defined for routine practice. The aim of this study was to define the length of L-dopa (L-3, 4-dihydrophenylalanine) and dopamine agonist monotherapy. The duration of monotherapy and discontinuation rates were investigated in a natural observational setting by plotting Kaplan-Meier survival curves. Out of 345 patients, 180 (52.2%) received L-dopa and 165 (47.8%) received a dopamine agonist as initial monotherapy. Half of the patients starting L-dopa received supplementary therapy with- in 3.6 years (95% confidence interval, 3.2-4.6), significantly longer than for dopamine agonist monotherapy (half required a second agent at 2.3 years [2.0-2.9]; P = 0.00017). Discontinuation of L-dopa therapy was 1%. Dopamine agonists were stopped (due to side-effects like impulse control disorders [6%], somnolence [4%] and light-headedness [3%]) in 20% over four years. The duration and tolerability of L-dopa and dopamine agonists as initial Parkinson's disease monotherapy are defined in this study; this may form part of the information exchange with patients.


Sujet(s)
Antiparkinsoniens/usage thérapeutique , Agonistes de la dopamine/usage thérapeutique , Lévodopa/usage thérapeutique , Maladie de Parkinson/traitement médicamenteux , Sujet âgé , Antiparkinsoniens/effets indésirables , Benzothiazoles/usage thérapeutique , Intervalles de confiance , Troubles du sommeil par somnolence excessive/induit chimiquement , Troubles du contrôle des impulsions/induit chimiquement , Sensation vertigineuse/induit chimiquement , Agonistes de la dopamine/effets indésirables , Association de médicaments , Femelle , Hallucinations/induit chimiquement , Humains , Indoles/usage thérapeutique , Estimation de Kaplan-Meier , Lévodopa/effets indésirables , Mâle , Adulte d'âge moyen , Pramipexole , Facteurs temps
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